A compound with the molecular formula C7H14O exhibits the following 13C NMR spectra: Broadband-decoupled 220 200 180 160 140 120 100 80 -0 DEPT-90 220 200 180 160 140 120 100 80 DEPT-135 220 200 180 160 140 120 100 9-9 60 40 40 20 909 60 40 20 80 60 40 20 Chemical Shift (ppm) Several structures are consistent with these spectra. To determine which structure is correct, a ¹H NMR spectrum was acquired which exhibits five signals. One of those signals is a singlet at 1.9 ppm with an integration of 3, and another of the signals is a doublet at 0.9 ppm with an integration of 6. Using this information, draw the correct structure of the compound. Draw Your Solution

A compound with the molecular formula C7H14O exhibits the following 13C NMR spectra: Broadband-decoupled 220 200 180 160 140 120 100 80 -0 DEPT-90 220 200 180 160 140 120 100 80 DEPT-135 220 200 180 160 140 120 100 9-9 60 40 40 20 909 60 40 20 80 60 40 20 Chemical Shift (ppm) Several structures are consistent with these spectra. To determine which structure is correct, a ¹H NMR spectrum was acquired which exhibits five signals. One of those signals is a singlet at 1.9 ppm with an integration of 3, and another of the signals is a doublet at 0.9 ppm with an integration of 6. Using this information, draw the correct structure of the compound. Draw Your Solution

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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